JP2007505148A5 - - Google Patents

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Publication number
JP2007505148A5
JP2007505148A5 JP2006526388A JP2006526388A JP2007505148A5 JP 2007505148 A5 JP2007505148 A5 JP 2007505148A5 JP 2006526388 A JP2006526388 A JP 2006526388A JP 2006526388 A JP2006526388 A JP 2006526388A JP 2007505148 A5 JP2007505148 A5 JP 2007505148A5
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JP
Japan
Prior art keywords
composition
composition according
alkyl
disease
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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JP2006526388A
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English (en)
Japanese (ja)
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JP4908215B2 (ja
JP2007505148A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2004/029942 external-priority patent/WO2005026112A2/en
Publication of JP2007505148A publication Critical patent/JP2007505148A/ja
Publication of JP2007505148A5 publication Critical patent/JP2007505148A5/ja
Application granted granted Critical
Publication of JP4908215B2 publication Critical patent/JP4908215B2/ja
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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JP2006526388A 2003-09-12 2004-09-13 疾患の治療法 Expired - Lifetime JP4908215B2 (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US50281103P 2003-09-12 2003-09-12
US60/502,811 2003-09-12
US53144303P 2003-12-19 2003-12-19
US60/531,443 2003-12-19
US56050904P 2004-04-07 2004-04-07
US60/560,509 2004-04-07
PCT/US2004/029942 WO2005026112A2 (en) 2003-09-12 2004-09-13 Methods of treating a disorder

Publications (3)

Publication Number Publication Date
JP2007505148A JP2007505148A (ja) 2007-03-08
JP2007505148A5 true JP2007505148A5 (enrdf_load_stackoverflow) 2007-11-08
JP4908215B2 JP4908215B2 (ja) 2012-04-04

Family

ID=34317479

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006526388A Expired - Lifetime JP4908215B2 (ja) 2003-09-12 2004-09-13 疾患の治療法

Country Status (6)

Country Link
US (1) US20050209300A1 (enrdf_load_stackoverflow)
EP (1) EP1677794B1 (enrdf_load_stackoverflow)
JP (1) JP4908215B2 (enrdf_load_stackoverflow)
CA (1) CA2538759C (enrdf_load_stackoverflow)
ES (1) ES2530972T3 (enrdf_load_stackoverflow)
WO (1) WO2005026112A2 (enrdf_load_stackoverflow)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7977049B2 (en) 2002-08-09 2011-07-12 President And Fellows Of Harvard College Methods and compositions for extending the life span and increasing the stress resistance of cells and organisms
US20060084135A1 (en) 2003-07-01 2006-04-20 Howitz Konrad T Compositions for manipulating the lifespan and stress response of cells and organisms
US20070105109A1 (en) * 2003-07-02 2007-05-10 Geesaman Bard J Sirt1 and genetic disorders
US20060074124A1 (en) * 2003-09-12 2006-04-06 Andrew Napper Methods of treating a disorder
US7446122B2 (en) * 2003-10-02 2008-11-04 Cephalon, Inc. Substituted indole derivatives
CA2550091A1 (en) * 2003-12-19 2005-07-07 Elixir Pharmaceuticals, Inc. Methods of treating a disorder
US8017634B2 (en) * 2003-12-29 2011-09-13 President And Fellows Of Harvard College Compositions for treating obesity and insulin resistance disorders
AU2004312072B2 (en) 2003-12-29 2011-06-23 President And Fellows Of Harvard College Compositions for treating or preventing obesity and insulin resistance disorders
CA2588389A1 (en) * 2004-11-23 2006-06-22 Ptc Therapeutics, Inc. Substituted phenols as active agents inhibiting vegf production
GB2422828A (en) * 2005-02-03 2006-08-09 Hunter Fleming Ltd Tricyclic cytoprotective compounds comprising an indole residue
AU2006218403A1 (en) * 2005-03-03 2006-09-08 Sirtris Pharmaceuticals, Inc. Fused heterocyclic compounds and their use as sirtuin modulators
WO2006138418A2 (en) 2005-06-14 2006-12-28 President And Fellows Of Harvard College Improvement of cognitive performance with sirtuin activators
WO2007047604A2 (en) * 2005-10-18 2007-04-26 Elixir Pharmaceuticals, Inc. Sirt1 inhibition
WO2008019825A1 (en) * 2006-08-14 2008-02-21 Santhera Pharmaceuticals (Schweiz) Ag Use of tricyclic indole derivatives for the treatment of muscular diseases
EP1891949A1 (en) * 2006-08-14 2008-02-27 Santhera Pharmaceuticals (Schweiz) AG Use of tricyclic indole derivatives for the treatment of muscular atrophy
JP2010523720A (ja) * 2007-04-12 2010-07-15 プレジデント アンド フェロウズ オブ ハーバード カレッジ β−カテニン関連疾患の処置のための、サーチュインに基づいた方法および組成物
WO2009099643A1 (en) * 2008-02-07 2009-08-13 The J. David Gladstone Institutes Use of sirt1 activators or inhibitors to modulate an immune response
AU2009333588A1 (en) 2008-12-08 2011-07-21 Northwestern University Method of modulating HSF-1
US20140249193A1 (en) * 2011-04-12 2014-09-04 The Regents Of The University Of California Modulators of mitochondrial protein import
AR088377A1 (es) * 2011-10-20 2014-05-28 Siena Biotech Spa Proceso para la preparacion de 6-cloro-2,3,4,9-tetrahidro-1h-carbazol-1-carboxamida y compuestos intermedios de esta
SG10201901192TA (en) * 2014-09-10 2019-03-28 Epizyme Inc Smyd inhibitors
WO2016094688A1 (en) 2014-12-10 2016-06-16 Massachusetts Institute Of Technology Fused 1,3-azole derivatives useful for the treatment of proliferative diseases
US10106555B2 (en) 2016-02-16 2018-10-23 Massachusetts Institute Of Technology Max binders as MYC modulators and uses thereof
WO2024236024A1 (en) 2023-05-16 2024-11-21 Aop Orphan Ip Ag Preparation of (s)-6-chloro-2,3,4,9-tetrahydro-1h-carbazole-1-carboxamide in enantiomerically enriched form by resolution process
AR132693A1 (es) 2023-05-16 2025-07-23 Aop Orphan Ip Ag Nuevos polimorfos de (s)-6-cloro-2,3,4,9-tetrahidro-1h-carbazol-1-carboxamida en forma cristalina

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3769298A (en) * 1971-04-02 1973-10-30 Pfizer Substituted aminomethylcarbazoles
BE793493A (fr) * 1971-12-30 1973-06-29 Hoffmann La Roche Composes tricycliques
DE2226703A1 (de) * 1972-05-25 1973-12-13 Schering Ag Neue tetrahydrocarbazolderivate und verfahren zu ihrer herstellung
US4009181A (en) * 1973-01-22 1977-02-22 Hoffmann-La Roche Inc. Cyclopenta[b]indole-2-carboxylic acids and derivatives thereof
BG25793A3 (bg) * 1973-07-18 1978-12-12 Schering Aktiengesellschaft Метод за получаване на карбазолови деривати
DE2431292A1 (de) * 1974-06-27 1976-01-15 Schering Ag Neue carbazol-derivate
CN1166169A (zh) * 1994-07-27 1997-11-26 三共株式会社 用作毒蕈碱性受体别构效应物的杂环化合物
JP2950433B2 (ja) * 1995-07-10 1999-09-20 インターナシヨナル・ビジネス・マシーンズ・コーポレーシヨン バッテリ収納装置
US5830911A (en) * 1996-08-14 1998-11-03 American Home Products Corporation Pyranoindole and tetrahydrocarbazole inhibitors of COX-2
AU2002315166A1 (en) * 2001-06-15 2003-01-02 The Trustees Of Columbia University In The City Of New York Sir2alpha-based therapeutic and prophylactic methods
MXPA04005768A (es) * 2001-12-14 2004-09-10 Zentaris Gmbh Derivados de tetrahidrocarbazol como ligandos para receptores acoplados a proteina g (gpcr).
AU2003214873A1 (en) * 2002-01-18 2003-09-02 Ceretek Llc Methods of treating conditions associated with an edg receptor

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